{
    "disease_id": "DOID:0060672",
    "recommended_name": {
        "id": "DOID:0060672",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060672",
        "name": "Grn-related frontotemporal lobar degeneration with Tdp43 inclusions",
        "description": "A frontotemporal dementia characterized by variable phenotypic expression typically including social, behavioral, or language deterioration, rather than memory or motor deficits and the presence of TARDBP-positive inclusions that has_material_basis_in mutation in the GRN gene on chromosome 17q21.31."
    },
    "synonyms": [
        {
            "id": "MONDO:0011842",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011842",
            "name": "Grn-related frontotemporal lobar degeneration with Tdp43 inclusions",
            "description": "A frontotemporal dementia characterized by variable phenotypic expression typically including social, behavioral, or language deterioration, rather than memory or motor deficits and the presence of TARDBP-positive inclusions that has_material_basis_in mutation in the GRN gene on chromosome 17q21.31."
        },
        {
            "id": "MONDO:0011842",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011842",
            "name": "frontotemporal dementia with Tdp43 inclusions, Grn-related",
            "description": ""
        },
        {
            "id": "MONDO:0011842",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011842",
            "name": "frontotemporal lobar degeneration with Tdp43 inclusions, Grn-related",
            "description": ""
        },
        {
            "id": "MONDO:0011842",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011842",
            "name": "frontotemporal dementia, ubiquitin-positive",
            "description": ""
        },
        {
            "id": "MONDO:0011842",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011842",
            "name": "frontotemporal lobar Degeneration with ubiquitin-positive inclusions",
            "description": ""
        },
        {
            "id": "MONDO:0011842",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011842",
            "name": "aphasia, primary progressive",
            "description": ""
        },
        {
            "id": "MONDO:0011842",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011842",
            "name": "dementia, hereditary dysphasic disinhibition",
            "description": ""
        },
        {
            "id": "MONDO:0011842",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011842",
            "name": "Ftld-TDP, Grn-related",
            "description": ""
        },
        {
            "id": "MIM:607485",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/607485",
            "name": "Ubiquitin-positive frontotemporal dementia",
            "description": "Ubiquitin-positive frontotemporal dementia"
        }
    ]
}